Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

HOSPAL BIOSPAL 1800S

K-Number: K863961 · 1986-12-17

Decision Date1986-12-17
Product CodeKDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HOSPAL BIOSPAL 1800S is the device name listed in this FDA 510(k) record. The listed applicant is Hospal Medical Corp.. It received FDA 510(k) clearance on 1986-12-17 under 510(k) number K863961. The device is classified under product code KDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOSPAL BIOSPAL 1800S?

HOSPAL BIOSPAL 1800S is a medical device that received FDA 510(k) clearance on 1986-12-17. The listed applicant is Hospal Medical Corp.. The 510(k) number is K863961.

When did HOSPAL BIOSPAL 1800S receive FDA 510(k) clearance?

HOSPAL BIOSPAL 1800S received FDA 510(k) clearance on 1986-12-17, under 510(k) number K863961.

Who is the listed applicant for HOSPAL BIOSPAL 1800S?

The FDA 510(k) record lists Hospal Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOSPAL BIOSPAL 1800S?

The FDA product code for HOSPAL BIOSPAL 1800S is KDI.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Hospal Medical Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 55 devices →

Related Devices (Code: KDI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑